NCT07204626

Brief Summary

Analyze the experience (perception, interpretation and incorporation - embodiment) that migrant people with low socio-economic status/precarity have of their own health conditions for which they have come to be hospitalized in the Intensive Care Unit (ICU) and Post-Resuscitation Rehabilitation Care (PRRC).

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
2mo left

Started Oct 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress75%
Oct 2025Jul 2026

First Submitted

Initial submission to the registry

September 24, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

October 2, 2025

Completed
13 days until next milestone

Study Start

First participant enrolled

October 15, 2025

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 15, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 15, 2026

Last Updated

October 2, 2025

Status Verified

May 1, 2025

Enrollment Period

9 months

First QC Date

September 24, 2025

Last Update Submit

September 24, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Exploration of the lived experience and perceptions of health and critical care among socio-economically vulnerable migrant patients hospitalized in intensive care units (ICU) and post-ICU rehabilitation units (SRPR), assessed through semi-structured int

    2 hours

Study Arms (2)

patient

medical staff

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study population will consist of adult migrant patients (≥18 years old) hospitalized in intensive care units (ICU) and receiving post-ICU rehabilitation care (SRPR) in selected French hospitals (Saint-Denis, Gonesse, Avicenne, Bichat). Eligible patients include those born outside France, regardless of their date of arrival, length of residence, or nationality, and who are able to communicate in French, Spanish, or Italian, either directly or via professional interpretation or cultural mediation. Participants must have a psychological and neurological state compatible with providing informed consent and participating in interviews.

You may qualify if:

  • For patients:
  • Male and female migrants (born outside of France and its territories, regardless of date of arrival, length of residence, or acquired nationality)
  • Aged 18 years or older
  • Living in or transiting through France
  • With or without residence permits or legal documentation
  • Hospitalized in ICUs and receiving care in post-ICU rehabilitation units (SRPR)
  • Providing consent to participate in the study
  • Having good proficiency in French, Spanish, or Italian, or, if not, benefiting from professional interpretation (ISM) or cultural mediation ensuring effective communication
  • Having a psychological and neurological state compatible with providing informed consent and taking part in an interview
  • For healthcare professionals and associative actors:
  • Being a healthcare, social work, or associative professional
  • Involved in the medical, psycho-social, and/or legal support and care of migrant patients admitted to ICUs and SRPR
  • Providing consent to participate in the study

You may not qualify if:

  • For patients:
  • Being born in France
  • Being a minor (\<18 years old)
  • Being under guardianship or curatorship
  • Having a neurological state incompatible with providing informed consent and taking part in an interview
  • For healthcare professionals and associative actors:
  • Not being involved in the care of migrant patients admitted to ICUs and SRPR

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre Hospitalier de Saint-Denis

Saint-Denis, France, France

Location

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
8 Months
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 24, 2025

First Posted

October 2, 2025

Study Start

October 15, 2025

Primary Completion (Estimated)

July 15, 2026

Study Completion (Estimated)

July 15, 2026

Last Updated

October 2, 2025

Record last verified: 2025-05

Locations